Evidence map›Paper›PMID 38464470›Full record

ArticleNeurosurgery practice2023

Phase 1, Dose Escalation, Nonrandomized, Open-Label, Clinical Trial Evaluating the Safety and Preliminary Efficacy of Allogenic Adipose-Derived Mesenchymal Stem Cells for Recurrent Glioblastoma: A Clinical Trial Protocol.

Andres Ramos-Fresnedo, Rawan Al-Kharboosh, Erin L Twohy, Aleeshba N Basil, Ewa C Szymkiewicz, Abba C Zubair, Daniel M Trifiletti, Nisha Durand, Dennis W Dickson, Erik H Middlebrooks and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Neurosurgery practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Human iPSC-Derived MSCs Induce Neurotrophic Effects and Improve Metabolic Activity in Acute Neuronal Injury Models.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Andres Ramos-FresnedoDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Rawan Al-KharbooshAtpoint tx, Washington, District of Columbia, USA.
Erin L TwohyAlliance Statistics and Data Center, Mayo Clinic, Rochester, Minnesota, USA.
Aleeshba N BasilDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Ewa C SzymkiewiczDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Abba C ZubairDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, Florida, USA.
Daniel M TrifilettiDepartment of Radiation Oncology, Mayo Clinic, Jacksonville, Florida, USA.
Nisha DurandCenter for Regenerative Biotherapeutics, Mayo Clinic, Jacksonville, Florida, USA.
Dennis W DicksonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, Florida, USA.
Erik H MiddlebrooksDepartment of Radiology, Neuroradiology Division, Mayo Clinic, Jacksonville, Florida, USA.
David N AbarbanelDepartment of Neurology, Neuro-Oncology Division, Mayo Clinic, Jacksonville, Florida, USA.
Stephany Y TzengDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Joao Paulo AlmeidaDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Kaisorn L ChaichanaDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Jordan J GreenDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Wendy J ShermanDepartment of Neurology, Neuro-Oncology Division, Mayo Clinic, Jacksonville, Florida, USA.
Alfredo Quiñones-HinojosaDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Jacksonville College · USMayo Clinic in Florida · USJohns Hopkins University · USMayo Clinic · US

Funding

Intra-Operative, Label-Free Detection of Brain Cancer Infiltration with Quantitative Optical ImagingR01CA200399 · NCI · JOHNS HOPKINS UNIVERSITY · PI LI, XINGDE, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$3.0M
Tumor targeted drug delivery nanoplatform to overcome therapy resistance glioblastomaR01NS129671 · NINDS · MAYO CLINIC JACKSONVILLE · PI DEBABRATA MUKHOPADHYAY · 2023 to 2026
$2.4M
A novel microfluidic device to predict brain cancer prognosis and response to therapyR01CA216855 · NCI · MAYO CLINIC JACKSONVILLE · PI KONSTANTOPOULOS, KONSTANTINOS, QUINONES-HINOJOSA, ALFREDO · 2018 to 2022
$2.4M
Nanoparticle Modified Human Fat Derived Mesenchymal Stem Cells for Brain Cancer (Change of Organization Application)R01CA195503 · NCI · MAYO CLINIC JACKSONVILLE · PI GREEN, JORDAN, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$1.9M
BMP4 Engineered Mesenchymal Stem Cell Therapy for GlioblastomaR01CA183827 · NCI · MAYO CLINIC JACKSONVILLE · PI QUINONES-HINOJOSA, ALFREDO · 2015 to 2019
$1.9M
Advanced Development of Desorption Electrospray Ionization Mass Spectrometry for Intraoperative Molecular Diagnosis of Brain Cancer using Pathology BiopsiesR33CA240181 · NCI · PURDUE UNIVERSITY · PI CHAICHANA, KAISORN LEE, COOKS, ROBERT GRAHAM · 2020 to 2021
$771k
NCI NIH HHS R01 CA183827NCI NIH HHS R01 CA195503NCI NIH HHS R01 CA200399NCI NIH HHS R01 CA216855NCI NIH HHS R33 CA240181NINDS NIH HHS R01 NS129671
6 · The paper itself

Abstract

Background and Objectives: Despite standard of care with maximal safe resection and chemoradiation, glioblastoma is the most common and aggressive type of primary brain cancer. Surgical resection provides a window of opportunity to locally treat gliomas while the patient is recovering, and before initiating concomitant chemoradiation. To assess the safety and establish the maximum tolerated dose of adipose-derived mesenchymal stem cells (AMSCs) for the treatment of recurrent glioblastoma (GBM). Secondary objectives are to assess the toxicity profile and long-term survival outcomes of patients enrolled in the trial. Additionally, biospecimens will be collected to explore the local and systemic responses to this therapy. Methods: We will conduct a phase 1, dose escalated, non-randomized, open label, clinical trial of GBM patients who are undergoing surgical resection for recurrence. Up to 18 patients will receive intra-cavitary application of AMSCs encapsulated in fibrin glue during surgical resection. All patients will be followed for up to 5 years for safety and survival data. Adverse events will be recorded using the CTCAE V5.0. Expected Outcomes: This study will explore the maximum tolerated dose (MTD) of AMSCs along with the toxicity profile of this therapy in patients with recurrent GBM. Additionally, preliminary long-term survival and progression-free survival outcome analysis will be used to power further randomized studies. Lastly, CSF and blood will be obtained throughout the treatment period to investigate circulating molecular and inflammatory tumoral/stem cell markers and explore the mechanism of action of the therapeutic intervention. Discussion: This prospective translational study will determine the initial safety and toxicity profile of local delivery of AMSCs for recurrent GBM. It will also provide additional survival metrics for future randomized trials.

Indexed as

Human Mesenchymal Stem CellsProspectiveStem CellStromal CellWindow of Opportunity

Identifiers

PMID38464470
PMCPMC10923529
OpenAlexW4394758151

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.